A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008833



Internal ID21918176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36096254..36096459hg38UCSC Ensembl
chr9:36096251..36096456hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584448
Samples
Known GenesRECK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008833
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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